arrow
返回

Accelerating read mapping with FastHASH

delete2013-01-21
delete99
delete
OA
AI
辛弘毅 封面图
辛弘毅 (Hongyi Xin)
D
Donghyuk Lee
F
Farhad Hormozdiari
S
Samihan Yedkar
O
Onur Mutlu *
C
Can Alkan
DOI:10.1186/1471-2164-14-S1-S13delete
delete原文链接
delete分享
delete收藏
查看原文
摘要

摘要

En 中文
With the introduction of next-generation sequencing (NGS) technologies, we are facing an exponential increase in the amount of genomic sequence data. The success of all medical and genetic applications of next-generation sequencing critically depends on the existence of computational techniques that can process and analyze the enormous amount of sequence data quickly and accurately. Unfortunately, the current read mapping algorithms have difficulties in coping with the massive amounts of data generated by NGS. We propose a new algorithm, FastHASH, which drastically improves the performance of the seed-and-extend type hash table based read mapping algorithms, while maintaining the high sensitivity and comprehensiveness of such methods. FastHASH is a generic algorithm compatible with all seed-and-extend class read mapping algorithms. It introduces two main techniques, namely Adjacency Filtering, and Cheap K-mer Selection. We implemented FastHASH and merged it into the codebase of the popular read mapping program, mrFAST. Depending on the edit distance cutoffs, we observed up to 19-fold speedup while still maintaining 100% sensitivity and high comprehensiveness.
Keyword:
SEGMENTAL DUPLICATIONS
COPY NUMBER
GENOME
EVOLUTION
ALIGNMENT
SEQUENCES
SEARCH
AI总结

AI总结

对已上传原文的论文进行重点信息的提取,主要内容包括:简要概述、研究摘要、背景介绍、关键亮点、图文解析、展望与总结。

期刊

BMC Genomics 封面图
BMC Genomics
IF:
3.7
论文数:
1.9W
被引数:
5.2W

机构

C
Carnegie Mellon University
学者数:
1.4W
论文数: 1.4W
被引数: 2.7W
U
university of california los angeles
学者数:
5.3W
论文数: 4.2W
被引数: 89
University of California System 封面图
University of California System
学者数:
37.7W
论文数: 33.8W
被引数: 6.6K
学者 查看更多机构
引用论文

引用论文

A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk16 p12.1处的大而复杂的结构多态性是微缺失疾病风险的基础
err2010-08-22
err91
errOAAI
errAntonacci, Francesca; Kidd, Jeffrey M.; Marques-Bonet, Tomas; Teague, Brian; Ventura, Mario; Girirajan, Santhosh; Alkan, Can; Campbell, Catarina D.; Vives, Laura; Malig, Maika; Rosenfeld, Jill A.; Ballif, Blake C.; Shaffer, Lisa G.; Graves, Tina A.; Wilson, Richard K.; Schwartz, David C.; Eichler, Evan E.
err分享
err收藏
Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays
err2000-06-01
err1.6K
PREAI
errBrenner, S; Johnson, M; Bridgham, J; Golda, G; Lloyd, DH; Johnson, D; Luo, SJ; McCurdy, S; Foy, M; Ewan, M; Roth, R; George, D; Eletr, S; Albrecht, G; Vermaas, E; Williams, SR; Moon, K; Burcham, T; Pallas, M; DuBridge, RB; Kirchner, J; Fearon, K; Mao, J; Corcoran, K
err分享
err收藏
mrsFAST: a cache-oblivious algorithm for short-read mapping
err2010-08-01
err261
errOAAI
errHach, Faraz; Hormozdiari, Fereydoun; Alkan, Can; Hormozdiari, Farhad; Birol, Inanc; Eichler, Evan E.; Sahinalp, S. Cenk
err分享
err收藏
Segmental duplications: Organization and impact within the current Human Genome Project assembly
err2001-05-08
err605
errOAAI
errBailey, JA; Yavor, AM; Massa, HF; Trask, BJ; Eichler, EE
err分享
err收藏
Hotspots of mammalian chromosomal evolution
err2004-03-08
err209
errOAAI
errBailey, JA; Baertsch, R; Kent, WJ; Haussler, D; Eichler, EE
err分享
err收藏
学者 查看更多内容